HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-Indazol-6-amine → HCID 135988978, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-Indazol-6-amine | HCID 81423 | — |
| Reactant | 1H-Indole-2,3-dione, 6-bromo- | HCID 95716 | — |
| Product | HCID 135988978 | HCID 135988978 | 48.1% |
Reaction Steps
The title compound (82 mg, 48%) was synthesized as a orange red solid according to the method described for Example A74 using 6-bromoisatin (113 mg, 0.5 mmol), 6-aminoindazole (73 mg, 0.55 mmol). 1H NMR indicated a 83:17 mixture of E/Z isomers. 1H NMR (400 MHz, DMSO-d6) δ 13.07 (s, 1H, NH), 10.93 (brs, 1H, NH), 8.09 (s, 1H), 7.84 (d, J=8.4 Hz, 1H), 7.08 (s, 1H), 7.05 (d, J=1.6 Hz, 1H), 6.92 (dd, J=8.0 Hz, 1.6 Hz, 1H), 6.77 (dd, J=8.4 Hz, 1.2 Hz, 1H), 6.27 (d, J=8.0 Hz, 1H); MS ESI 341.1 [M+H]+, calcd for [C15H9BrN4O+H]+ 341.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08765748B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-9db4c5681a454d07bc7acf989564ceca |
| Source note | uspto-grants-2014_07 |